Acute Right Ventricular Infarction Registry

NCT06424028 | Recruiting

• 1 other identifier: IRB-62/2023
• Study Type: observational
• Target: 1,000
• Locations: 1 country
• Sites: 1

Brief Summary

This Study aims to provide an assessment of clinical presentation, management, hospital course, and prognosis of acute right ventricular infarction presenting with or without Inferior or infero-posterior wall Myocardial Infarction and the assessment of composite adverse clinical outcome after reperfusion in-hospital and post-discharge (in 30 Days Prognosis).

Conditions

Inferior Wall; Transmural Myocardial Infarction; Right Ventricular Dysfunction

Outcome Measures

Primary Outcomes (1)

• Composite adverse clinical outcome

  Atleast one adverse event, such as pump failure, cerebrovascular accident (CVA), stent thrombosis, major bleeding, contrast-induced nephropathy (CIN), ventricular arrhythmias, or mortality.

  Upto 30 days from admission

Interventions

Right Ventricular Infarct OTHER

Consecutive patients presented with isolated inferior, infero-posterior and inferolateral wall MI with or without acute right ventricular infarction.

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patients presented at a tertiary care hospital with Inferior and posterior wall MI with and without RV infarction undergoing PPCI who are fulfilling the eligibility criteria will be enrolled.

You may qualify if:

• Patients of Inferior, infero-lateral and infero-posterior wall MI with and without RV infarction undergoing PPCI.
• Both male and female patients.
• Patients of age ≥ 18 years.

You may not qualify if:

• Patients who will not give consent for participation.

Sponsors & Collaborators

• National Institute of Cardiovascular Diseases, Pakistan: lead

Study Sites (1)

National Institute of Cardiovascular Diseases

Karachi, Sindh, 75510, Pakistan

RECRUITING

MeSH Terms

Conditions

Ventricular Dysfunction, Right

Condition Hierarchy (Ancestors)

Ventricular Dysfunction; Heart Diseases; Cardiovascular Diseases

Study Officials

• Rajesh Kumar, MBBS, FCPS

  National Institute of Cardiovascular Diaseses

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Rajesh Kumar, MBBS, FCPS

CONTACT

+923337306090; rajeshnarsoolal@gmail.com

Musa Karim, MSc

CONTACT

03323646169; mkarim.nicvd@gmail.com

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Target Duration: 30 Days
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Associate Professor Adult Cardiology

Study Record Dates

• First Submitted: May 10, 2024
• First Posted: May 21, 2024
• Study Start: January 20, 2024
• Primary Completion: July 19, 2024
• Study Completion: August 19, 2024
• Last Updated: May 21, 2024

Record last verified: 2024-05

Data Sharing

• IPD Sharing: Will not share

Locations

PA (1)